欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2400/002
药品名称Azitromycine Auro 500 mg, film-coated tablets
活性成分
    • azithromycin dihydrate 500.0 mg
剂型Film-coated tablet
上市许可持有人Aurobindo Pharma B.V. Baarnsche Dijk 1 3741 LN Baarn
参考成员国 - 产品名称Netherlands (NL)
Azitromycine Actavis 500 mg, film-coated tablets
互认成员国 - 产品名称
    • Slovakia (SK)
      Azithromycin Actavis 500 mg
    • Denmark (DK)
      Azitromycin Actavis
    • Iceland (IS)
      Azithromycin Actavis 500 mg filmuhúðuð tafla
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • Latvia (LV)
      Azithromycin Actavis 500 mg apvalkotās tabletes
    • Lithuania (LT)
      Azithromycin Actavis 500 mg plėvele dengtos tabletės
    • Estonia (EE)
      AZITHROMYCIN ACTAVIS
    • Hungary (HU)
      Zitinn 500mg filmtabletta
许可日期2012/08/21
最近更新日期2021/12/08
药物ATC编码
    • J01FA10 azithromycin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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